Determinants of Bacteriophage 933W Repressor DNA Binding Specificity

PLoS One

Daniel Samorodnitsky¹  Rayna C. Rosati¹  Gerald B. Koudelka¹  Tammy J. Bullwinkle¹ 

[1] Department of Biological Sciences, University at Buffalo, Buffalo, New York, United States of America

关键词: DNA-binding proteins;    DNA sequence analysis;    Sequence motif analysis;    Electrophoretic mobility shift assay;    Guanine;    DNA structure;    Sequence alignment;    DNA cleavage;   

DOI  :  10.1371/journal.pone.0034563

学科分类：医学（综合）

来源: Public Library of Science

【 摘 要 】

We reported previously that 933W repressor apparently does not cooperatively bind to adjacent sites on DNA and that the relative affinities of 933W repressor for its operators differ significantly from that of any other lambdoid bacteriophage. These findings indicate that the operational details of the lysis-lysogeny switch of bacteriophage 933W are unique among lambdoid bacteriophages. Since the functioning of the lysis-lysogeny switch in 933W bacteriophage uniquely and solely depends on the order of preference of 933W repressor for its operators, we examined the details of how 933W repressor recognizes its DNA sites. To identify the specificity determinants, we first created a molecular model of the 933W repressor-DNA complex and tested the predicted protein-DNA interactions. These results of these studies provide a picture of how 933W repressor recognizes its DNA sites. We also show that, opposite of what is normally observed for lambdoid phages, 933W operator sequences have evolved in such a way that the presence of the most commonly found base sequences at particular operator positions serves to decrease, rather than increase, the affinity of the protein for the site. This finding cautions against assuming that a consensus sequence derived from sequence analysis defines the optimal, highest affinity DNA binding site for a protein.

【 授权许可】

CC BY